Product Recalls in Tennessee
Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,670 recalls have been distributed to Tennessee in the last 12 months.
Showing 8541–8560 of 29,188 recalls
Recalled Item: Medical Device products purchased from Family Dollar retail stores located...
The Issue: Potential exposure to rodents and rodent activity in the distribution center.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Mount Clamp Assembly (table adapter component) Recalled by Deerfield...
The Issue: Reports have been received that after normal or routine lateral forces are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIPOSORBER System Recalled by Kaneka America Corp Due to Labeling change to...
The Issue: Labeling change to due to the risk of severe anaphylactoid reactions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter IRISpec CA/CB/CC control Recalled by Beckman Coulter, Inc....
The Issue: IRISpec CA failures for glucose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene Recalled by Meridian Bioscience Inc Due to The photomultiplier...
The Issue: The photomultiplier tube, may have compromised functionality in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProteusPLUS and ProteusONE- designed to produce and deliver a proton...
The Issue: When resuming from a beam pause, the Proton Therapy System does not verify...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evita V500 Ventilator with Software 2.51.01 and Lower - intended Recalled by...
The Issue: Cybersecurity Improvement Action-not equipped against potential cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Recalled by...
The Issue: IFU update includes an update to the Device description, Intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Celect PlatinumVena Cava Filter Set Catalog Number/GPN:...
The Issue: IFU update includes an update to the Device description, Intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babylog VN500 Ventilator with Software 2.51.01 and Lower- intended for...
The Issue: Cybersecurity Improvement Action-not equipped against potential cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cytocell 8 Square Template Slides (Glass)- microscope slides : PCN008...
The Issue: Labelled with an incorrect expiry date on the outer label with an extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compella Therapy Air Supply Unit Recalled by Baxter Healthcare Corporation...
The Issue: Potential damage to the power cord may cause the power conductors to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compella Bariatric Bed System Recalled by Baxter Healthcare Corporation Due...
The Issue: Potential damage to the power cord may cause the power conductors to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.1 (709031) Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: While performing a fluoroscopy examination, there is a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.0 (709030) Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: While performing a fluoroscopy examination, there is a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUNTLEIGH Disposable intraoperative Probe Recalled by Huntleigh Healthcare...
The Issue: Faceplate may become detached from the probe body.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4-11B Recalled by RaySearch America Inc Due to Incorrect source...
The Issue: Incorrect source to skin or surface distance (SSD) calculation may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Integrated Reaction Units (IRU) Recalled by Abbott Molecular, Inc....
The Issue: There is potential for the Reaction Vessels (RVs) detaching from the RV cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.